A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6458706



Internal ID21116259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:93048132..93065472hg38UCSC Ensembl
chr12:93441908..93459248hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg3817341
hg1917341
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185373
Samples
Known GenesLOC643339
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6458706
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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